Molecular basis of combined pituitary hormone deficiencies. - Wikidata - awgldk - TriplyDB

Molecular basis of combined pituitary hormone deficiencies.

Molecular basis of combined pituitary hormone deficiencies.

http://www.wikidata.org/entity/Q34146692

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Over- and underdosage of SOX3 is associated with infundibular hypoplasia and hypopituitarism A novel dominant negative mutation of OTX2 associated with combined pituitary hormone deficiency Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54 Borjeson-Forssman-Lehmann syndrome: a novel pituitary phenotype due to mutation in a novel gene Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humans Dynamic interactions between Pit-1 and C/EBPalpha in the pituitary cell nucleus.Magnetic resonance imaging of the hypothalamus-pituitary unit in childrensuspected of hypopituitarism: who, how and when toinvestigate.Mechanisms for pituitary tumorigenesis: the plastic pituitary.GATA2 mediates thyrotropin-releasing hormone-induced transcriptional activation of the thyrotropin β gene.The use of neuroimaging for assessing disorders of pituitary development.Atrazine binds to the growth hormone-releasing hormone receptor and affects growth hormone gene expression Research resource: T-antigen transformation of pituitary cells captures three novel cell lines in the Pit-1 lineage.NR4A1 (Nur77) mediates thyrotropin-releasing hormone-induced stimulation of transcription of the thyrotropin β gene: analysis of TRH knockout mice.Novel insights into the aetiology and pathogenesis of hypopituitarism.Genetics, gene expression and bioinformatics of the pituitary gland.Magnetic resonance imaging of sellar and juxtasellar abnormalities in the paediatric population: an imaging review.Three Japanese patients with congenital pituitary hormone deficiency and ophthalmological anomalies.Inherited adrenal hypoplasia: not just for kids!Growth hormone in chronic renal disease.Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency Hypopituitarism and Legg-Calve-Perthes disease related to difficult delivery.Thyroglobulin gene mutations and other genetic defects associated with congenital hypothyroidism.Molecular basis of adrenal insufficiency.Growth hormone deficiency and combined pituitary hormone deficiency: does the genotype matter?Sexual precocity: a historical perspective and update.The role of transcription factors implicated in anterior pituitary development in the aetiology of congenital hypopituitarism.Neuronal M3 muscarinic acetylcholine receptors are essential for somatotroph proliferation and normal somatic growth.Rare Frequency of Mutations in Pituitary Transcription Factor Genes in Combined Pituitary Hormone or Isolated Growth Hormone Deficiencies in Korea.Growth hormone treatment in adults with growth hormone deficiency: the transition.Identification and biological characterization of chicken embryonic cardiac progenitor cells.Pituitary size fluctuation in long-term MR studies of PROP1 deficient patients: A persistent pathophysiological mechanism?The role of growth hormone in determining birth size and early postnatal growth, using congenital growth hormone deficiency (GHD) as a model.Prolactinoma through the female life cycle.Hypothalamus-Pituitary-Thyroid Axis.Laterality disturbance and hypopituitarism. A case report of co-existing situs inversus totalis and combined pituitary hormone deficiency.Molecular analysis of PROP1, PIT1, HESX1, LHX3, and LHX4 shows high frequency of PROP1 mutations in patients with familial forms of combined pituitary hormone deficiency.Heterozygous mutation of HESX1 causing hypopituitarism and multiple anatomical malformations without features of septo-optic dysplasia.The c.301_302delAG PROP1 gene mutation in Romanian patients with multiple pituitary hormone deficiency.A novel germline mutation, IVS4+1G>A, of the POU1F1 gene underlying combined pituitary hormone deficiency.

P2860

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P2860

Molecular basis of combined pituitary hormone deficiencies.

http://www.wikidata.org/entity/Q34146692

description

2002 nî lūn-bûn

@nan

2002 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2002 թվականի օգոստոսին հրատարակված գիտական հոդված

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2002年の論文

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2002年論文

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2002年論文

@zh-hant

2002年論文

@zh-hk

2002年論文

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2002年論文

@zh-tw

2002年论文

@wuu

name

Molecular basis of combined pituitary hormone deficiencies.

@ast

Molecular basis of combined pituitary hormone deficiencies.

@en

Molecular basis of combined pituitary hormone deficiencies.

@nl

type

label

Molecular basis of combined pituitary hormone deficiencies.

@ast

Molecular basis of combined pituitary hormone deficiencies.

@en

Molecular basis of combined pituitary hormone deficiencies.

@nl

prefLabel

Molecular basis of combined pituitary hormone deficiencies.

@ast

Molecular basis of combined pituitary hormone deficiencies.

@en

Molecular basis of combined pituitary hormone deficiencies.

@nl

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Endocrine Reviews

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Molecular basis of combined pituitary hormone deficiencies.

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Laurie E Cohen

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Sally Radovick

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431-442

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scholarly article

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10.1210/ER.2001-0030

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4

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23

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2002-08-01T00:00:00Z

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12202459

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